4 months symptoms and conditions

I'm a 38 y/o woman. For 7 yrs I knew my cholesterol has been high. I refused to take cholesterol medication and decided to diet and exercise but that didn't work. I've had 2 children in the past 3 yrs. In May of this year I started having chest pains and palpitations. I had blood tests done. I was given Inderal and also prescribed Zocor 20mg for my cholesterol. It was 243 with and LDL of 178. I took Zocor for a week. I felt so awful. I was weak, I lost my appetite. I was constantly tired. I couldn't even carry my 10 month old son, yet alone care for him. I informed my physician and she changed it to Lipitor 20mg. I thought I was doing fine. I checked my levels again after a month. My cholesterol was 113 and LDL 58. I trusted the doctor knew what she was doing. At the same time I also was taking Omega 3's. I asked my doc to lower the dosage to 10mg. From the time I was taking Zocor and the start of Lipitor. I was feeling tingling and numbness in my arms, hands, fingers, toes, feet and legs. I also was having muscle pain. I asked my doctor about that. She mentioned because of my heart palpitations, it could be symptoms of anxiety and panic. I had feeling of pins and needles throughout my body, not knowing when it would occur. I had muscle pain in my arms and legs and neck pain. I went online to see the side effects of Lipitor and came across this website. I decided to do an experiment. I stopped taking Lipitor 9 days ago. I was on statins for almost 4 months. I don't have the feeling of tingling and numbness, but I still have pins and needles and muscle pain. I have to say, I feel so much better. I hope to get better. I 'd really like to know, how long does the medication stay in your system? What are the effects of getting off it so suddenly. I'd love to feel myself again.

So i told you I would post an update from my gyno... so here it is (below is my original post)

I went to the doctor and her nurse asked me if i had a little bit of cramping and i said yeah its actually off to the side, and she said that i might have some sort of blockage by my ovaries.... well then my doctor came in and she said that everything was perfectly normal. and decided to put me onto yaz... well i'm not going to take it. and it worries me that i might have a blockage. I took out the ring last night and it is gone for good! I can't wait to get back to my normal self. i am going to see how i do this month without the ring and still see if i have the cramps if i do i will go back if not then we can just assume it was caused from nuva....

August 15th
2008
12:14 AM

So I got on NuvaRing because I needed something with low hormones that wouldn't make me crazy like other BC's. I've been on it for almost 3 years now and didn't start having problems until recently. Now I get night sweats... i wake up and i am soaking wet from sweat, depressed, cry and get angry for no reason. Like the other night I was in the middle of eating dinner and i just started balling uncontrollably for no reason. My sex drive really hasn't decreased all that much it's still there; but i have discharge like there is no tomorrow and sometimes it smells. I figured if i douched that would help the situation but apparently not. I also haven't had a "period" in like 4 months and i'm not pregnant. I say "period" because NuvaRing doesn't allow your ovaries to ovulate so it's not really a period but withdrawal blood because your not shedding any uterine lining.I also recently have had bad migraines... thinking that having my wisdom teeth finally removed would take care of that issue but it's been 3 months since that and the answer is no. I have no energy to do anything all i want to do is sleep but i hate sleeping because i wake up soaking wet from sweat. It bothers me when my husband and I have sex and hurts. I also can not go a day without taking pepto; my stomach hurts even if i drink water. don't get me wrong i love the fact that i've lost weight but not because my stomach hurts too much to eat. I know if your looking for something to help you pin point what it is i'm sorry that you're not getting it from me. But I can tell you this after a while you get tired of it. I am going to talk to my gyno to see what my other options are. I can't take it any longer and neither can my husband. I have never PMSed as bad as I have been lately. If you're experiencing any of these I would recommend you call your gyno/dr and let them know; there could be something better for you out there. Sometimes I wonder why we woman put our bodies through these things. If all else fails looks like we'll just be going back to the old school days of condoms and spermicide lube. i'll post in a few days after my gyno apt to let you know what she said about my symptoms... but you'll know when you've had enough.

My son has been taking Singular for a few years for mild asthma and recently in the past few months all of the sudden he has been having a hard time falling asleep,anxiety at bedtime taking hours to get to sleep with me having to stay in the room. We took him to his pediatrician who ran blood tests and referred me to a sleep specialist who suggested he may have OCD or Anxiety. I just thought it was just something that would pass after 4 months it still has not passed. I am removing him from Singular TODAY. After all these visits with these doctors who knew he was on the medication and never said anything to me about possible side effects . I cant believe it took an article my husband saw in the paper for this to come to my attention.

Hi I am 33 and has had a bilateral tubal ligation (cauterization) and I a have stopped having a regular monthly cycle for the last 2 years My doctor prescribed this BC for me over a year ago, however I did not fill the prescription. But about a month ago my period finally came after being absent for about 4 months. It was very heavy, bleeding through my clothes and feeling weak. After having my period for about 2 weeks I decided to go to my obgyn to get some help, she gave me provera for 5 days to stop the bleeding and said that I should take the yaz to regulate it. The provera stopped the bleeding for 3 days then I started to bleed again. She said that was normal. I started the yaz about 9 days ago, and began to feel very sick. I wanted to vomit all the time, my head hurt like crazy, I became very moody, restless in the night when its time to go to bed and ends up staying up all night. I ended up missing days from work and when I did go in I would leave early. I decided to stop taking it and for the last two days have felt better. However I have started bleeding again. I really don't know what to do but I don't think I want to continue taking any form of BC.

I have used the NuvaRing for about 3.5 years, starting after my 6 week check up when my daughter was born in 2004. In the beginning I felt like it decreased my sex drive but also that maybe post baby body that caused that too. For three years I had no problems. I had noticed breast tenderness throughout but other than that no side effects. About 8 months ago it began with a missed period, then two periods in one month. My OBGYN recommended 'resetting' my body by taking out the ring until my next cycle and starting it up again. I followed his directions but the next cycle came along with a bladder infection followed by a yeast infection. Over the next 4 months I either had one or the other, continually visiting my doctor I didn't make any connection to the two. Stomach pain, chronic fatigue and kidney pain also added to the list. My doctor prescribed a series of medications followed by blood tests and a referral to a specialist. Over the summer my husband asked that I stop using the ring because my sex drive had hit rock bottom. After a few weeks of taking out the ring, the burning sensation during urination has gone away. Stomach cramps and back pain has ceased and no infection to date. I am in my early thirties and after a week off the ring I realized what they mean by 30's sex drive. My husband and I are both happy with the changes. I visit my OBGYN again in a few weeks to revisit non-hormone options for BC

I've been taking Fosamax once a week for about 4 months. During that time what began-before taking Fosamax-as mild pain in my lower back-has gotten progressively worse. This is the only negative possible symptom I’ve experienced, but of late it has increased and spread to my hips. I decided to stop taking it today, and see if it makes any difference. If it does, I will post another reply here with details.

I think all reading these personal accounts should consider this: obviously many medical professionals see far more benefit than loss in the majority of users. My osteoporosis was only diagnosed via a bone scan 6 months ago. -2.5 The increased pain and worsening conditions in my back might in fact be much worse if I hadn’t started taking the Fosamax. One must beware of apophenia setting in with self diagnosis.

Most posting here already had serious medical needs to have Fosamax prescribed in the first place, given a small percentage of diagnostic errors. Most of the conditions I’ve seen described vary greatly, and without a serious study are purely antidotal. I suspect there are legitimate adverse reactions, but for now the percentage and severity remains a big unknown. There seem to be some activists here, so get a campaign going for publicly funded analysis of the now considerable amount of data on file.

If my back gets better, I’ll still be unsure as it might have been a delayed benefit from the drug. Likely I will take Fosamax again either way. If it doesn’t improve in several months I’ll assume F-max wasn’t the cause and begin taking it again. If it gets better, I will take F-max again to see if the problems return when I do. If they don’t I’ll keep taking it. If they do, that will red-line my ‘coincidence meter’ and I’ll never touch the stuff again.

I hope some will find my approach to our common dilemma helpful. We all have to be our own advocates within the modern health care cabal. I worry about the old adage that when we do so, we have a fool for a client. Feel free to criticize my reasoning, and thanks to all the others that took the time to share your experience. It helped me make my decision, and I’ll share the results in about 6 months.

I am a 54 year old male who started taking Lipitor about 4 years ago. It seemed OK at first, but over the next several years I began to have increasing amounts of joint pain after exercise. Nor muscle pain, joint pain. And it seemed to be a result of exercise. By the time I stopped it, I was hurting after everything, not just exercise. I felt better within the first two weeks, but it took about 4 months for me to be able to exercise vigorously again. Over the years I seemed to have forgotten how much vitality I used to have. I am a physician, and because of the long lag time until I felt better, I wondered whether improvement might have related to other factors, so after about 5 months I decided to restart Lipitor. It surprised me that after just one dose, I got back all of the joint pain and fatigue when I was at my worst on Lipitor. I was really hurting. Needless to say, I didn't take any more.

Coincidentally, a physician friend of mine who had statin induced polyneuropathy had a similar experience. After his symptoms went away he found that after only one dose the entire polyneuropathy came back.

Stopping and restarting the drug is a way to test the correlation between the drug and the side effect. For such a large spectrum of side effects to recur after only a single dose, it argues that the problems that my friend and I had was due to some sort of immune memory response. I have not seen this in the medical literature.

I am off it now for about 8 months and am able to comfortably play singles tennis and jog - much more energy (and I took 200 mg of CoQ10 a day with the Lipitor).

my husband has been on plavix for about 6 months. He had a heart attack and had a couple stents. He also was a drug addict hut he quit for 4 months he was doing good. unfortunately he started using again (methamphetamines) he also started drinking alcohol not a good combination. I was always telling him that he is trying to kill himself. Well he was feeling great according to him and he felt great, well just yesterday hi went to the restroom and he said that his urine had blood clot and blood. He said the doctor told him he had to quit using meth he said he swore he would. I'm not sure if he is telling me everything or if there is more to this. Has anyone wad blood clots in there urine? I understand these circumstances are different my husband being a drug addict but i need some help is it more than what he is telling me.

i am 26 years old and i had my daughter 5/3/2008, at my 6 week i had mirena put in because of the wonderful idea of not having to worry about taking a pill! the day i had it put in i bled like i was on the heaviest period i've every had and i continued to bleed for the next 7 weeks. every day i would at least have one bright, red gush of blood, one day i even had cramping so bad that it felt like labor.... i had a HORRIBLE labor! this wasn't how it was supposed to be, my sister came over to watch my daughter while i curled up in ball for about 4 hours until i took my last loratab from giving birth!!!! i had a strange pain in my left leg daily that ran from my groin area to my knee, i had severe depression to the point that i stopped breast feeding, was so irritated with anything and everything and i cried every day. i hadn't done this while pregnant or the first 6 weeks at all!! i lost all of my baby weight in about 2 weeks after giving birth ( i only gained 17lbs ) but since having mirena put in i've gained at least 7 lbs back. my stomach bloated up so huge it looked like i was 4 months pregnant, even when i would shower and rubbed the soap on my my belly it was very tender to the touch. i also suffer from ibs and with mirena i have never had such horrible, horrible stomach aches and constantly going to the bathroom.needless to say i had it removed 4 weeks ago and the very same day my mood changed dramatically and the bleeding stopped. the weight isn't going anywhere though which makes me sad although i think a good, daily cardio workout will help that. i'm still losing a lot of hair, i'm a hair stylist so i know to expect some, but it's pretty extreme. my stomach is still a little bloated but it is improving and no longer hurts to the touch and the ibs has improved dramatically .... i think every woman should be well warned on what's involved with this drug, do your research. i DO NOT recommend this to anyone, it is not worth the pain and depression. having a newborn is hard enough and adding all of these side effects made me feel like my very stable, loving home and family was falling apart. DO NOT GET THIS PUT IN YOUR BODY!

OMG- I wish I had read this before I had this thing put in. Its been in about 4 months, I bled for 6 weeks after having it put in (which was painful), my cramps during that time felt like someone was stabbing me (worse then labor pains) I lost so much of my hair, which is coming back ( I thought the hair loss was from the after pregnancy) that I still have a receding hairline. The bottoms of my feet always hurt, my stomach always looks bloated and I cant loose the extra 10 pounds (which I gained after having it put in) I have absolute NO DRIVE, feel depressed all the time, feel no pleasure in anything that I cant even enjoy my infant son. My boyfriend calls me crazy and unstable because I am so moody. WOW, I am calling to make an appointment to have this taken out ASAP

When my son was 6mos old I had the Mirena placed. I had spotting for about 6 weeks (which I was informed would probably happen so I wasn't too upset about that.) The 4th month of having the Mirena I started getting severe anxiety, mood swings and bloating. I also have an itchy, flaky scalp that started around 3 or 4 months after placement. I never made the connection that all of this could be caused from the Mirena until today when I had it removed because my husband and I want to have another child. After I had it removed I went home and took a nap. Literally, 2 or 3 hours after it was removed I felt like myself again. I was on the verge of an emotional break down and didn't know why...and I just thought I had better pick myself up and quit whining. It felt like my life was spiraling out of control but nothing external was happening to make me feel so panicked all of the time. I thought it was an odd coincidence that I felt better all a sudden. That's what prompted me to check online to see if anyone else had experienced this. Anyway, after I read a lot of the entries I felt relieved and hopeful to continue to feel like myself again.

I'm a physician. Usually Kenalog injections can be avoided and oral steroids used like prednisone. The local dimpling effect may occur if the injection is too shallow, actually there is a temporary "disolving" of the subcutaneous tissue, the muscle and joints are not damaged. It is usually viewed as a "cosmetic" adverse effect. The Kenalog injections was primarily designed for joint injection and the kenalog or similar depo form stays active in the joint for a few weeks. All steroid medications can cause irritability and this is usually temporary for a few days. Steroids can cause muscle weakness- this is usually associated with high doses for prolonged use like being on prednisone for 3 or 4 months. Steroids can have an adverse effect on menstruation, but this is usually associated with chronic use. The most serious problems with the steroids result in bone weakness(osteoporosis) and serious damage to joints like the back and hip. Steroids can also result in weight gain, diabetes, high blood pressure and cataract formation. I don't think Kenalog is any different than other steroids such as Medrol or Prednisone in terms of the side effect profile. These are dangerous medications that can also be very helpful in saving lives and diminishing pain.

I've had Mirena for about 14 months now. Yeah, I HATE it.
The day they put it in, I was in the category where it took forever to place. Like 3-4 tries to place it. Thank God I'd had experience in handling this type of pain, having 2 children w/out epidurals.

I bled for 6 weeks straight, so the day I went for my follow-up, I stopped bleeding. Figures. I'm looking at the brochures in the office for a different type of contraceptive. The doctor thinks I'm stupid, why would I want to do that? Um, because it pokes my husbands penis head and I can see the red poke marks on it. So the doc trims the tail and loses a piece of it somewhere inside me. CRAZY!

The following month, I really started having low back pain. Then I herniate my L-5. I'm not sure that any of that is related to the IUD. Just speculating. Also speculation, I battled with thrush the entire 13 months I nursed my son. That was never the case with my first child.

So I go about a year with out a period that I can really speak of. Maybe some spotting, but I haven't thought about the thing much. Although, I don't remember ever having a positive thought about it. I could feel it during sex. I can't explain that feeling, but, it's like I could feel it poking my husband at times.

Now, I am having some CRAZY stomach bloat and I'm extremely exhausted. My back is still constantly hurting me. I'm spotting ALL the time. Mostly brown blood, though. Does that mean it's old blood? Every time I have sex, I will spot within the 2nd day. I've held off going to get it removed simply because I don't have insurance and am not looking to get pregnant again. However, I know that it needs to be done. There is something wrong inside me. I never had the weight gain issues other women had. But I am up 5 pounds right now and my belly looks to me like I'm 4 months prego. Matter of fact, I'll probably take a home test tomorrow so I don't have to pay for one at the GYNO.

Anybody know much about getting pregnant with an IUD? And why are doctors so gung-ho for IUD's? Is it because they are like $2000?

Thank god I found this web site!!! I have had the Mirena in for 4 months now! So I'm not going crazy as well! I have been experiencing the same side affects: awful Headaches days & weeks on end, no sex drive , moody, Depressed, stomach pain, just not feeling like my self! etc. I wanted to have the paraguard put in, but was pressured into getting the mirena! terrible choice!! I called today to make a appointment to get this thing out ASAP!! Why aren't these company's required to do more testing on this crap! They don't care about people's health they just want to make a buck!!

I am a 39 year old female and I had an atrial ablation a 2 years ago, then 4 months later the a-fib returned and I went on the flecainide. I have nw been on the flecainide for more that a year 150mg(am) and 100mg(pm) and the shortness of breath and flutter has returned. Has anyone else had anything like this happen to them?

I have been reading all of these posts and have another question. I hope that someone can help. My daughter, 8 years old, has been on Singulair since she was 4. She is normally a very happy girl with a wonderful disposition. For the last year or so, she has been having trouble getting herself to sleep at night. She says that she hears things in her head such as ringing or "noises". A few hours before she knows it's bedtime, she cries and when we ask her why she's crying, she can't give us a reason. We initially thought that she was crying for no reason because she didn't want to go to sleep. I remember reading about the side effects of Singulair causing mood swings, etc., but her's are not violent mood swings. Just very emotional and has a hard time coming down from the "episode". I'm at a loss...I have not talked to her doctor yet about it, but have told her that we will make an appointment this week to discuss it with him. My husband suggested that maybe it sounded like she was having a panic attack or anxiety attack. I hate to label her as that at such a young age. My mind now goes back to the side effects of Singulair and maybe this is to blame. Any help or suggestions would be greatly appreciated. Thank you! Concerned Mom

This is an evil drug, far more dangerous than most illegal drugs. It ruined my life. I wish I had never been put on it. It was the first drug I, a teenager, was put on, having just been diagnosed with my disease.

I hadn't tried other drugs or other treatments; medical guidelines, I know now, say not to use this drug unless the disease is both severe and other treatments have failed. Well, I hadn't tried other treatments yet, so I shouldn't have been put on this drug. And yet the doctor I was assigned, Dr. Anne Sullivan at the University of Iowa's hospital, thought I needed to be on it, told me it was safe, that it didn't have any side effects, and that I would be completely healthy again in a few weeks.

If I had been told about the side effects, as doctors are supposed to do, according to both legal and medical standards, if my doctor had honestly answered my questions about side effects, I never would've taken it. And I'd advise others to never take this terrible drug. I would rather die than take this drug again.

It did nothing for my disease, but it did give me quite a few side effects, some which, according to the doctors I've subsequently went to, are permanent and long-lasting and there's nothing you can do about them; they're just permanent.

People don't talk about the psychological effects of steroids, but they should; they're serious. And, no, they don't just go away when you stop taking the drug. If the drug makes you bipolar, you're not just going to just go back to being you're regular self. Bipolar disorder, depression, anxiety, these things don't just go away on their own.

I had no problem with mental illness before taking this drug, and yet I'm still severely depressed to this day, part of that, perhaps, is from what the drug did to me, that is, the physical side effects, but part of, I suspect, is just that it changed my personality, like it changed my brain chemistry.

Go here-******to learn about the psychiatric effects of prednisone.

Excerpts:

"Although a powerful therapeutic option, corticosteroids are associated with serious adverse effects, both physiologic and psychiatric. While the somatic adverse effects of corticosteroid therapy (Table 1) have been extensively researched and widely described, the neuropsychiatric adverse effects have received less attention."

"In our literature review, we found that the potential psychiatric adverse effects of corticosteroids span a symptom spectrum from subtle mood changes to full-blown affective syndromes and frank psychosis."

"The most commonly reported corticosteroid-induced psychiatric disturbances are affective, including mania, depression, or mixed states."

"Cognitive deficits, particularly declarative or verbal memory deficits, have been well documented during both long- and short-term corticosteroid therapy."

"More severe cognitive impairment consistent with delirium or dementia has also been described."

"In a case-control study of 20 patients receiving long-term low-dose corticosteroid therapy (prednisone, 7.5 mg/d for >6 months) and 14 volunteers with similar illnesses who were not receiving corticosteroid therapy, Bolanos et al9 found a 60% lifetime risk of corticosteroid-induced mood or anxiety disorder."

"The corticosteroid dosage is the most important risk factor for the development of psychiatric symptoms."

"Psychiatric disturbances can occur at any point during corticosteroid treatment, including almost immediately after initiation and even after cessation of treatment."

"Corticosteroid-induced psychiatric disturbances are common and include mania, depression, psychotic or mixed affective states, cognitive deficits, and minor psychiatric disturbances (irritability, insomnia, anxiety, labile mood)."

"It is important that clinicians in all specialties become aware of the potential psychiatric adverse effects associated with corticosteroids and explain these effects to their patients."

"Which patients will experience corticosteroid-induced psychiatric disturbances cannot be predicted. Dosage is the most important risk factor for the development of adverse effects, with patients receiving less than 40 mg/d at minimal risk, those taking 40 to 80 mg/d at moderate risk, and patients receiving more than 80 mg/d at high risk. Most patients will develop symptoms during the first week of treatment, and more than 90% will develop symptoms by 6 weeks."

Side effects: mixed bipolar disorder/manic-depression, suicidal ideation, cystic acne, scars on my face, panic attacks, severe anxiety, rage, euphoria, sadness, impulsiveness, confusion, memory loss, hard to concentrate and remember, thin skin, delayed healing ability, bruises, premature aging, rapid heart beat, heart palpitations, high blood pressure, higher cholesterol, thyroid disease, sweating all over, itching all over, joint pain, increased appetite, massive weight gain, stretch marks, hormones out of balance now, dry eyes, so dry my eyelids stick to my eyes, so dry I can't wear contacts any more, permanent red eyes, blurry vision, vision worsened, eye pain, eyes sensitive to light, migraines, and yellow skin.

My son became soo aggressive 3 days after starting Singulair, that he was almost banned from soccer for life because of attacking another player on the field. It resembled what I had heard of 'roid rage'. When I questioned the doctor immediately, was told there was no connection. After months of the aggression, then came depression and self mutilation. My 15 yr old was secretly burning himself to 'punish' himself for things he done wrong or "disappointing" those around him. He now has permanent scars all over his arms from these burns. The depression took to drug abuse and my A student fell to an F student in 6 weeks. He completely lost his will to live and thrive. After 4 months of hell, the dr informed us that the FDA just warned physicians of this side effect. Im furious now that I read through the court documents and find that the drug company knew this all along. I know I am a luckier parent than some whose children committed suicide, but still wish that the FDA would get off their BUTTS and do something to take this drug off the market. I was told by a rep at the FDA that Merck will not take it off the shelf until they're made to because even if they had to pay parents millions for their child's suicide, they would still be pocketing more profit than our children's lives are worth in the court system. Not sure WHY we even HAVE an FDA, they won't do anything to protect us from these money hungry drug companies. A YEAR to do an 'INVESTIGATION" are you kidding me? If the CEO of Merck had to bury his child, it would come off the shelf THAT DAY.

I have been on Loestrin24 for about 4 months now, i am ending my pack today. Ive found that i have become very emotional towards my boyfriend and parents, i was on Yaz previous to this and i thought the yaz was not working for me but then i discovered when i went onto loestrin the yaz was fine, i found that with this pill i have extreme break outs on my face that i never had before besides the occasional ones around my period now i feel like they come all the time. My breast were randomly sore in the middle of the month and i was worried that i was pregnant. After reading all of these side effects from everyone else i have decided to go back on the Yaz.

I'm a 30 year old woman and I've been taking Yasmin for 4 months now. I've been reading what people have been posting here and I'm wondering if I'm alone in having the following symptoms:
-severe breast pain for one day in the middle of my cycle, followed by mild breast pain until I get my period,
-painful cramps in the middle of my cycle,
-weird sharp internal vaginal pain, (sorry for the graphics, but especially during climax),
-acne problems,
-depression
The last two, I did see that people wrote about on here. I called my doctor today and I'm requesting a new pill. I thought that after a couple of months the symptoms would equalize, but after this last month, I decided I couldn't live with it. The breast pain especially has been very painful.

I started using the Ring 2yrs ago, and at age 38 thought it was the best birth control for me, however within 2 to 3 days after putting it in I had extreme low pelvic back pain,and then within the 1st month, mood changes, fatigue, depression, no sex drive at all But somehow 3 months after being on it I got pregnant. Now I am 40yrs and started the Nuvaring again about 4 months ago and have all the horrible side effects as before. I don't know why I let my Gyn talk me into again. I am now experiencing major pains in my left leg, which I have never had such pain in my leg before at all. And I believe it is the symptom of having blood clots. Which is one of the side effects that is listed. I will be going to the Doctor ASAP to check this out. So anyone else that is having any type of pain in the leg, even if it feels like a ingrown hair bothering you or a little pinch feeling or burning sensation here and there, Go have it checked out before its to late and it becomes painful and possibly a blood clot.

I had the Mirena placed in on July 27, 2008 - as the weeks went on, I started to get dizzy a lot, BLURRY vision - I did not connect the two. I've been bleeding now for almost three weeks and I called the doctor because of that and she wants to see me on Friday. What also is happening is my stomach is VERY bloated that I feel like I am 4 months pregnant (and I have 2 kids - so I know what that feels like), I have terrible acne all of a sudden and oily skin and itchy scalp that I just want to scratch my head so hard.... is it me getting older or is it this thing??!!!?!?!?

I am now weaning off of Wellbutrin after 4 months - I was taking it to quit smoking (I had just been through a very stressful divorce and I was smoking way more than normal.) I did not experience most of what has been discussed here (negative side effects) except for mild headaches. I am posting this simply to tell the few people who have experienced the headaches that I believe this will go away. I (like a dummy) told myself I'd only take 150mg a day rather than the whole 300mg my doctor had prescribed. This didn't work - I needed the whole 300mg, taken at 150mg doses at exactly 12 hour intervals (this makes a huge difference!) About two weeks after beginning this med, I experienced feelings of euphoria (which were quite pleasant!) but feel like I balanced out within a month. One other side effect was a change in menstrual cycle - I'm normally exactly 28 day-predictable, but missed every other month in the four months I've been on this (coincidence? Not sure...) I also drink beer nearly every night (2-4 bottles, sometimes none, sometimes more) and never had any type of seizures. Bottom line...this drug definitely helped me cut way back on smoking - I am a stress smoker and since this alleviated my stress, I didn't smoke hardly at all. Now that I'm weaning off (and yes, I did cut pills in half and have not experienced anything bad) I am curious to see if my desire to smoke will return.

Just wanted to post this out there for anyone who has had similar side effects. Overall, I have been very happy with this drug (but have never taken other Anti Depressants, so can't compare with others).

I have been taken diovan now for about 4 months and I have no complaints. on last week my doctor switch me to lisinop/hctz but after reading all the negative responses i rather continue paying the high cost medication.

I have asthma that was not controlled. I coughed and wheezed constantly. I had trouble eating, because even the food passing through the esophagus was enough to cause an attack. I was in and out of the emergency room for years, and the Ambulance folks knew to arrive with epinephrine when I'd call.

I started taking Singulair sometime around 1998. I haven't had any serious problems since then with asthma, and have had ZERO side effects.

Every drug has side effects for some people. For me, Claritin causes my heart to race. I can take that or that purple circurlar inhaler thing. I had a terrible reaction to that.

For ME, Singulair works. I am not sure it should be given to children if they are having severe problems. But it certainly should NOT be removed from the market...because people like me needed it to control their asthma.